Canonical Allele Identifier: CA1929349888

Gene: CYP2C9

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.94989125A= , CM000672.2:g.94989125A=	GRCh38
NC_000010.10:g.96748882A= , CM000672.1:g.96748882A=	GRCh37
NC_000010.9:g.96738872A=	NCBI36
NG_008385.1:g.55468A=
NG_008385.2:g.55968A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260682.8:c.*97A= MANE Select	ENSP00000260682.6:n.*97A=
ENST00000643112.1:c.*579A=	ENSP00000496202.1:n.*579A=
ENST00000260682.6:c.*97A=	ENSP00000260682.6:n.*97A=
NM_000771.3:c.*97A=	NP_000762.2:n.*97A=
NM_000771.4:c.*97A= MANE Select	NP_000762.2:n.*97A=